Clinical Trials Directory

Trials / Completed

CompletedNCT05882760

Postoperative Sensitivity Following Placement with Different Restorative Materials in Vital Posterior Teeth

Comparison of Postoperative Sensitivity Following Placement with Different Restorative Materials in Vital Posterior Teeth

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
160 (actual)
Sponsor
Liaquat University of Medical & Health Sciences · Academic / Other
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

There is a lack of long-term clinical studies comparing different restorative materials; most of the available studies have only looked at class I cavities or examined post-operative sensitivity in non-caries cervical lesions. The purpose of this study is to measure postoperative sensitivity in clinical settings at 3-month intervals for class 1 and 2 direct posterior restoration

Conditions

Interventions

TypeNameDescription
DRUGTetric N Bond Universal®Cavities will be restored with Conventional Hybrid Composite Restoration bonded with Etch \& Rinse Tetric - N - Bond (Ivoclar)
DRUGSelf Etch Tetric N Bond Universal®Cavities will be restored with Conventional Hybrid Composite Restoration bonded with Self Etch Tetric N Bond Universal®
DRUGGC Fuji IX, GC, Japan®Cavities will be restored with GC Fuji IX, GC, Japan®
DRUGActiva TM Bioactive Restorative ®Cavities will be restored with Activa TM Bioactive Restorative ®

Timeline

Start date
2023-06-01
Primary completion
2024-09-30
Completion
2024-12-31
First posted
2023-05-31
Last updated
2025-03-06

Locations

1 site across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT05882760. Inclusion in this directory is not an endorsement.